MINNEAPOLIS--(BUSINESS WIRE)--Jan. 17, 2007--MGI PHARMA, INC.
(Nasdaq:MOGN), a biopharmaceutical company focused in oncology and
acute care, today announced publication of data from a randomized,
double-blind, placebo-controlled phase 3 trial of Saforis(TM)
(glutamine) Powder in UpTec(TM) for Oral Suspension in the journal
Cancer. Results of this study, which were first presented at the
American Society of Clinical Oncology (ASCO) 2004 Annual Meeting,
indicate that treatment with Saforis significantly reduced the
incidence of severe oral mucositis when compared to placebo.
Saforis is an investigational therapy for the treatment and
prevention of oral mucositis in patients receiving mucotoxic cancer
therapy. Results of this phase 3 study formed the foundation for the
Saforis New Drug Application (NDA). MGI PHARMA received an approvable
letter for Saforis from the U.S. Food and Drug Administration (FDA) in
October 2006. Based on the FDA's request for an additional phase 3
trial, the Company is currently evaluating options to maximize the
value of Saforis.
The pivotal phase 3 trial of Saforis was conducted in 326 patients
with breast cancer who were receiving anthracycline-based chemotherapy
regimens. Patients in this trial were randomized to receive Saforis or
placebo during their first chemotherapy cycle. After their first
treatment cycle was complete, study participants were then crossed
over to receive the alternate treatment during their next cycle of
chemotherapy.
The primary endpoint of this trial, defined as a reduction in
incidence and severity of oral mucositis, was met. Data from this
study indicate that the incidence of World Health Organization (WHO)
Grade 2 or higher oral mucositis was significantly reduced in
Saforis-treated patients compared to patients who received placebo
(38.7 percent versus 49.7 percent; p=0.026). Among those patients that
experienced oral mucositis in this study, the incidence of severe oral
mucositis (WHO Grade 3 or higher) was significantly lower in the
Saforis arm compared with the placebo arm (1.2 percent versus 6.7
percent; p=0.005).
Overall, the data indicated that the safety profile of Saforis was
comparable with that of placebo. The most frequently-observed adverse
events considered possibly or probably related to the study drug were
nausea and dry mouth. No patient experienced a serious adverse event
while receiving Saforis.
About Oral Mucositis
Oral mucositis, a common side effect of mucotoxic cancer therapy,
is characterized by painful ulcerations, redness and swelling in the
mouth, which can cause difficulty swallowing and eating. It is
estimated that approximately 35% of patients undergoing mucotoxic
cancer therapy develop significant oral mucositis, which equates to
more than 200,000 patients per year. In addition to being difficult
for patients to manage, oral mucositis can interfere with a patient's
ability to continue their cancer therapy and may lead to an increased
risk of infection. It is also associated with higher healthcare
expenses as a result of frequent opioid analgesics used to manage
mucositis-related pain, emergency room visits due to complications
from oral mucositis and prolonged hospital stays.
About Saforis(TM) (glutamine) Powder in UpTec(TM) For Oral
Suspension
Saforis(TM) (glutamine) Powder in UpTec(TM) for Oral Suspension is
a product candidate for the prevention and treatment of oral mucositis
that occurs as a result of mucotoxic cancer therapy. Saforis has not
been approved for marketing by the U.S. FDA or any other regulatory
agency. An oral formulation of glutamine delivered via MGI PHARMA's
proprietary UpTec(TM) system, Saforis is designed to deliver high
concentrations of glutamine into damaged oral mucosa in order to
prevent damage from mucotoxic cancer therapies and to promote healing.
Although glutamine is the most abundant amino acid in human plasma,
the availability of and demand for glutamine becomes critical when
oral mucosa has been injured as a result of chemotherapy or radiation.
By directly exposing the oral mucosa to increased concentrations of
this important amino acid, Saforis may prevent damage to and promote
healing of the lining of the mouth.
About MGI PHARMA
MGI PHARMA, INC. is a biopharmaceutical company focused in
oncology and acute care that acquires, researches, develops and
commercializes proprietary products that address the unmet needs of
patients. MGI PHARMA markets Aloxi(R) (palonosetron hydrochloride)
Injection, Dacogen(TM) (decitabine) for Injection and Gliadel(R) Wafer
(polifeprosan 20 with carmustine implant) in the United States. MGI
PHARMA directly markets its products in the U.S. and collaborates with
partners to reach international markets. For more information, please
visit www.mgipharma.com.
This news release contains certain "forward-looking" statements
within the meaning of the Private Securities Litigation Reform Act of
1995. These statements are typically preceded by words such as
"believes," "expects," "anticipates," "intends," "will," "may,"
"should," or similar expressions. These forward-looking statements are
not guarantees of MGI PHARMA's future performance and involve a number
of risks and uncertainties that may cause actual results to differ
materially from the results discussed in these statements. Factors
that might cause MGI PHARMA's results to differ materially from those
expressed or implied by such forward-looking statements include, but
are not limited to, the ability of MGI PHARMA to continue to increase
sales of its marketed products, the ability to successfully
commercialize Saforis(TM) / the ability for MGI PHARMA to respond to
the FDA's approvable letter, the successful completion of clinical
trials for the Company's other product candidates, and other risks and
uncertainties detailed from time to time in MGI PHARMA's filings with
the Securities and Exchange Commission including its most recently
filed Form 10-K and Form 10-Q. MGI PHARMA undertakes no duty to update
any of these forward-looking statements.
CONTACT: MGI PHARMA, INC.
Jennifer Davis, 212-332-4381
IR@mgipharma.com
or
Susan Silao, 212-332-4364
SOURCE: MGI PHARMA, INC.